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  2. Progressive cardiac conduction disease
  3. CLCA2
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Progressive cardiac conduction disease

Gene: CLCA2

Amber List (moderate evidence)
CLCA2 (chloride channel accessory 2)
EnsemblGeneIds (GRCh38): ENSG00000137975
EnsemblGeneIds (GRCh37): ENSG00000137975
OMIM: 604003, Gene2Phenotype
CLCA2 is in 1 panel

1 review

Ivone Leong (Genomics England Curator)

I don't know

New gene submitted on behalf of the GMS Cardiology specialist group. The group has agreed that this gene should be Amber on this panel.
Created: 2 Dec 2019, 10:38 a.m. | Last Modified: 2 Dec 2019, 10:38 a.m.
Panel Version: 0.30
Created: 2 Dec 2019, 10:38 a.m.
Last Modified: 2 Dec 2019, 10:38 a.m.
Panel version: 0.30

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Amber
  • NHS GMS
Phenotypes
  • Heart conduction disease, MONDO:0000992
OMIM
604003
Clinvar variants
Variants in CLCA2
Penetrance
None
Panels with this gene

History Filter Activity

2 Mar 2021, Gel status: 2

Set Phenotypes

Ivone Leong (Genomics England Curator)

Phenotypes for gene: CLCA2 were changed from to Heart conduction disease, MONDO:0000992

2 Dec 2019, Gel status: 2

Created, Added New Source, Set mode of inheritance

Ivone Leong (Genomics England Curator)

gene: CLCA2 was added gene: CLCA2 was added to Progressive cardiac conduction disease. Sources: NHS GMS,Expert Review Amber Mode of inheritance for gene: CLCA2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown